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Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813860/ https://www.ncbi.nlm.nih.gov/pubmed/33462232 http://dx.doi.org/10.1038/s41467-020-20726-8 |
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author | Song, Li Pan, Junfeng Yang, Yantao Zhang, Zhenxing Cui, Rui Jia, Shuangkai Wang, Zhuo Yang, Changxing Xu, Lei Dong, Tao G. Wang, Yao Shen, Xihui |
author_facet | Song, Li Pan, Junfeng Yang, Yantao Zhang, Zhenxing Cui, Rui Jia, Shuangkai Wang, Zhuo Yang, Changxing Xu, Lei Dong, Tao G. Wang, Yao Shen, Xihui |
author_sort | Song, Li |
collection | PubMed |
description | Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show that the pathogen Yersinia pseudotuberculosis uses a T6SS (T6SS-3) to secrete a nuclease effector that kills other bacteria in vitro and facilitates gut colonization in mice. The effector (Tce1) is a small protein that acts as a Ca(2+)- and Mg(2+)-dependent DNase, and its toxicity is inhibited by a cognate immunity protein, Tci1. As expected, T6SS-3 mediates canonical, contact-dependent killing by directly injecting Tce1 into adjacent cells. In addition, T6SS-3 also mediates killing of neighboring cells in the absence of cell-to-cell contact, by secreting Tce1 into the extracellular milieu. Efficient contact-independent entry of Tce1 into target cells requires proteins OmpF and BtuB in the outer membrane of target cells. The discovery of a contact-independent, long-range T6SS toxin delivery provides a new perspective for understanding the physiological roles of T6SS in competition. However, the mechanisms mediating contact-independent uptake of Tce1 by target cells remain unclear. |
format | Online Article Text |
id | pubmed-7813860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78138602021-01-25 Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties Song, Li Pan, Junfeng Yang, Yantao Zhang, Zhenxing Cui, Rui Jia, Shuangkai Wang, Zhuo Yang, Changxing Xu, Lei Dong, Tao G. Wang, Yao Shen, Xihui Nat Commun Article Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show that the pathogen Yersinia pseudotuberculosis uses a T6SS (T6SS-3) to secrete a nuclease effector that kills other bacteria in vitro and facilitates gut colonization in mice. The effector (Tce1) is a small protein that acts as a Ca(2+)- and Mg(2+)-dependent DNase, and its toxicity is inhibited by a cognate immunity protein, Tci1. As expected, T6SS-3 mediates canonical, contact-dependent killing by directly injecting Tce1 into adjacent cells. In addition, T6SS-3 also mediates killing of neighboring cells in the absence of cell-to-cell contact, by secreting Tce1 into the extracellular milieu. Efficient contact-independent entry of Tce1 into target cells requires proteins OmpF and BtuB in the outer membrane of target cells. The discovery of a contact-independent, long-range T6SS toxin delivery provides a new perspective for understanding the physiological roles of T6SS in competition. However, the mechanisms mediating contact-independent uptake of Tce1 by target cells remain unclear. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7813860/ /pubmed/33462232 http://dx.doi.org/10.1038/s41467-020-20726-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Song, Li Pan, Junfeng Yang, Yantao Zhang, Zhenxing Cui, Rui Jia, Shuangkai Wang, Zhuo Yang, Changxing Xu, Lei Dong, Tao G. Wang, Yao Shen, Xihui Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title | Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title_full | Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title_fullStr | Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title_full_unstemmed | Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title_short | Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties |
title_sort | contact-independent killing mediated by a t6ss effector with intrinsic cell-entry properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813860/ https://www.ncbi.nlm.nih.gov/pubmed/33462232 http://dx.doi.org/10.1038/s41467-020-20726-8 |
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